Search results for "ONCE"

showing 10 items of 4997 documents

Milchsäure-Bildung und Verteilung in Erythrozytenkonzentraten

2001

chemistry.chemical_compoundAnesthesiology and Pain MedicinechemistryEmergency MedicineDistribution (pharmacology)General MedicineFood scienceCritical Care and Intensive Care MedicineRed cell concentrateLactic acidains · Anästhesiologie · Intensivmedizin · Notfallmedizin · Schmerztherapie
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Effects of non-ionic micelles on transient chaos in an unstirred Belousov-Zhabotinsky reaction.

2001

The behaviour of the Ce(IV)-catalyzed Belousov-Zhabotinsky (BZ) system has been monitored at 20.0 degrees C in unstirred batch conditions in the absence and presence of different amounts of the non-ionic micelle-forming surfactants hexaethylene glycol monodecyl ether (C10E6) and hexaethylene glycol monotetradecyl ether (C14E6). The influence of the non-ionic surfactants on both the kinetics of the oxidation of malonic acid (MA) by Ce(IV) species and the behaviour of the BZ reaction in stirred batch conditions has also been studied over a wide surfactant concentration range. The experimental results have shown that, in unstirred batch conditions, at surfactant concentrations below the critic…

chemistry.chemical_compoundAqueous solutionBelousov–Zhabotinsky reactionChromatographyPulmonary surfactantChemistryInduction periodCritical micelle concentrationKineticsAnalytical chemistryEtherPhysical and Theoretical ChemistryMicelleFaraday discussions
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1976

A radical mechanism is proposed for the formation of the 1,2-polymer 2 in the “spontaneous” polymerization of 4-vinylpyridinium salts 4-VP.HX (X=NO3, ClO4, HSO4, I) in aqueous solution on the basis of strong inhibition by oxygen and other radical inhibitors. Quantitative investigation of the influence of oxygen on the formation of the 1,2-polymer allowed the derivation of a formal kinetic scheme for the initiation and polymerization steps which is consistent with a free radical mechanism. Dependence of the average molecular weight of 2 on monomer concentration is in agreement with this model. Dependence of the inhibition time on the oxygen concentration as well as an acceleration of the fin…

chemistry.chemical_compoundAqueous solutionMonomerchemistryPolymerizationKineticsPolymer chemistrychemistry.chemical_elementMolar mass distributionLimiting oxygen concentrationOxygenPeroxideDie Makromolekulare Chemie
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Determination of fluoride in rocks, soils, and fluoride-bearing minerals by separation using direct distillation in sulfuric acid medium and spectrop…

1989

Abstract An analytical method for fluoride determination in geological samples is proposed. It is based on a previous fluoride separation by distillation with a Teflon reactor. The variables that influence distillation quantitation (temperature, time, and acid concentration) are optimized. The influence of some species on fluoride recovery during distillation are studied, and conditions to avoid this influence are suggested. Fluoride determination is carried out by means of a spectrophotometric method [La(III)-F−-Alizarin complexone system] (N. T. Crosby, A. L. Dennis, and J. G. Stevens, Analyst (London), 1968, 93, 643–652). The method is applied to the analysis of soils, rocks, and fluorid…

chemistry.chemical_compoundChromatographyAcid concentrationChemistrylawSoil waterSulfuric acidDistillationFluorideSpectroscopyAnalytical Chemistrylaw.inventionMicrochemical Journal
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Stability of 11-Nor-Δ9-carboxy-tetrahydrocannabinol Glucuronide in Plasma and Urine Assessed by Liquid Chromatography-Tandem Mass Spectrometry

2002

Abstract Background: Unconjugated 11-nor-Δ9-carboxy-tetrahydrocannabinol (THCCOOH) in blood and urine has been proposed as a valuable marker, but the glucuronide (THCCOOglu) is present in considerably higher concentrations than the parent drug. Acyl glucuronides have been shown to be potentially reactive conjugates, which may affect the in vitro metabolite pattern. Methods: Extraction procedures and a liquid chromatography-tandem mass spectrometry assay were developed and validated to investigate the stability of THCCOOglu in urine and plasma. Plasma and urine samples with added THCCOOglu were stored at −20, 4, 20, and 40 °C up to 10 days. Results: The glucuronide was stable at −20 °C in bo…

chemistry.chemical_compoundChromatographyMolar concentrationChemistryLiquid chromatography–mass spectrometryMetaboliteBiochemistry (medical)Clinical BiochemistryBlood plasmaCannabinolUrineGlucuronideMass spectrometryClinical Chemistry
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Viskosimetrische molekulargewichtsbestimmung von cellulose in kupfer-äethylendiamin

1955

Cellulose lost sich in Kupferathylendiamin („Cuen”) schneller und ist gegen Luftsauerstoff betrachtlich unempfindlicher als in Cuoxam. Im Gegensatz zu amerikanischen und franzosischen Arbeiten wurde festgestellt, das Losefahigkeit und Viskositatszahl weitgehend unabhangig von der Zusammensetzung des Komplexes und seiner Kupfermolaritat sind. Es wird eine Methode angegeben zur einfachen Herstellung einer Kupferathylendiaminlosung. Die viskosimetrischen Polymerisationsgr adbestimmungen von Cellulose in Cuen konnen unter Anwesenheit von Luft im Ostwald viskosimeter durchgefuhrt werden. Die dabei eryhaltenen Viskositatszahlen sind fur alle Cellulosematerialien um den Faktor 1,54 groser als die …

chemistry.chemical_compoundConcentration dependenceChemistryIntrinsic viscosityPolymer chemistryCelluloseDie Makromolekulare Chemie
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Monomeric vs. polymeric bonded iminodiacetate silica supports in high-performance ligand-exchange chromatography

1983

The synthesis of monomeric and polymeric bonded iminodiacetate-groups on silica supports is described. The polymeric support offers advantages over the monomeric, such as (i) preparation is much simpler, (ii) higher surface concentration of functional groups can be achieved without loss of efficiency and (iii) hydrolytic stability. Cu2+ loaded supports were examined for their kinetic performance, in particular for the C-parameter of the Knox equation, and for their hydrolytic stability. Calculation of the surface coverage shows that only a rather thin polymeric layer is formed; this is in agreement with the results of the kinetic performance. The retention of α-amino acids on the Cu2+ loade…

chemistry.chemical_compoundHydrolysisMonomerChromatographychemistryLigandOrganic ChemistryClinical Biochemistrymacromolecular substancesSurface concentrationBiochemistryLayer (electronics)Analytical ChemistryChromatographia
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Hemiesters and hemiamides of maleic and succinic acid: synthesis and application of surfactants in emulsion polymerization with styrene and butyl acr…

1999

Hemiesters and hemiamides of maleic acid with different chain lengths of the hydrophobic alkyl group (R = C8H17, C10H21, C12H25, C16H33) have been synthesized and used as surfactants in the emulsion polymerization of styrene and butyl acrylate. The same polymerization experiments were also carried out using nonreactive surfactants with an analogous succinic structure. The chemical structure of the surfactants was confirmed by 1H nuclear magnetic resonance. The melting point and critical micelle concentration of the reactive surfactants described herein were measured. All of the surfactants studied provided good stability of styrene/butyl acrylate latexes, when compared with a reference late…

chemistry.chemical_compoundMaterials sciencePolymers and PlasticsMaleic acidchemistryPolymerizationSuccinic acidButyl acrylateCritical micelle concentrationPolymer chemistryCopolymerEmulsion polymerizationStyrenePolymers for Advanced Technologies
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Rapid fluorimetric assay for primary amine groups in water samples

2003

Bond Elut C(18) solid-phase extraction cartridges were used for pre-concentration followed by derivatization with o-phthaldialdehyde-N-acetylcysteine (OPA-NAC) of primary amines in water. Optimal conditions were: conditioning the cartridges with borate buffer pH 10.4, retention of the primary amines, addition of the OPA-NAC(3.7 mmol L(-1)) 1:1 molar ratio and borate buffer pH 8, elution of the isoindol with MeOH-borate buffer (9:1) pH 10.2 and fluorescence measurement. The equations of the calibration graphs for methylamine, ethylamine, propylamine, butylamine, pentylamine, and beta-phenylethylamine at lambda(excitation)=330 nm and lambda(emission)=440 nm, in the optimal conditions are pres…

chemistry.chemical_compoundMolar concentrationChromatographyChemistryButylamineMethylamineFluorescence spectrometryPropylamineSolid phase extractionPentylamineDerivatizationBiochemistryAnalytical ChemistryAnalytical and Bioanalytical Chemistry
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Die Beschleunigung der Polymerisation durch Hydroperoxyd und Aminsalz

1964

Di-n-butylaminhydrochlorid vergrosert die Geschwindigkeit der durch Tetralinhydroperoxyd initiierten Polymerisation von Styrol und von Methylmethacrylat. Im Bereich kleiner Konzentrationen von Hydroperoxyd und Aminsalz bis zu je etwa 5·10−4 Mol/l ist die Reaktionsgeschwindigkeit der Wurzel aus der Hydroperoxyd- und Aminsalzkonzentration jedoch der Monomerkonzentration direkt proportional. The polymerisation rate of styrene and methylmethacrylate initiated by tetraline hydroperoxide is accelerated by di-n-butylamine hydrochloride. In the range of low concentrations up to 5 · 10−4 mole/l. of each, hydroperoxide and amine salt, the rate of polymerisation is proportional to the square roote of …

chemistry.chemical_compoundMonomerPolymerizationchemistryHydrochloridePolymer chemistryAmine gas treatingVolume concentrationStyreneDie Makromolekulare Chemie
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